As part of our Gaun Yersel! stories, Jane Holt reflects on ten years of the Self Management Strategy for Scotland.

There has been an unprecedented amount of change in how our health service is working: we have more people living longer, multimorbidity is the new normal, and we now have Health and Social Care Partnerships designed to shift the balance of care for acute hospitals to communities.

Hi-tech care is sexy and portrayed by the media in so many programmes like 24 hours in A&E. By contrast, although self management may not be viewed a fast or sexy, it is fundamental in giving people back a life worth living.

Despite working in an era of savings and financial scrutiny, if you put your head above the parapet, there are opportunities out there. For our team it was the Integrated Care Fund. We saw there was money available to work differently. Before, we were simply a cardiac rehab team, but we had a vision. If we could be a multimorbidity team we could increase access and availability to rehabilitation and self management for more people affected by long term conditions.

Did it make sense? Yes. Was there evidence for it? No.

We created HARP (Healthy and Active Rehabilitation Programme) for people affected by multiple long term conditions. Its approach embraces supported self management.

Under our new model, we wanted to work with a wider range of people other than cardiologists, specialist teams and people like “us”, important as these people are. We wanted to work with the Third sector, service users, Health and Social Care Partnerships, and link workers. We wanted seamless transitions with leisure services as well as shared training and meetings. This means that our new services are based in local communities in rural and deprived areas.

We are trying new activities with our service users like walking football, all ability cycling, and guest lecturing at further education events. We don’t think that we have to have all the answers, but we can help people to find their local solutions.

Building in peer support

In our previous world, we used to meet as medical professionals who always had to have the answers. It has been a total eye opener to see our service users come back as volunteers in our classes. They provide peer support, a realistic role model, and a lived experience. Our service users find them inspirational. Our activity friend volunteers have become valued team members and we wouldn’t want to work without them. They are the icing on our cake.

Living with chronic conditions – who cares?

The modern world can be a lonely place. Many of our service users describe a life where in the past they were living at home and did not go out. They felt they had lost their role as mum, brother, worker, or friend because they thought of themselves as an ill person. They had ruled out life through fear of making their medical conditions worse.

Rehabilitation with medical expertise, peer support, physical activity, information, hints and tips all contribute to finding a new normal. Good quality self management programmes with clinical expertise should be available for all people in local communities using co-productive principles to empower individuals and collectives.

Are we there yet? No. We are in our fourth year of building an evidence base, we are working with pots of funding, and awaiting secure posts for staff. But it is a blast and an adventure, and we aim to secure and embed this work not just locally, but to have it given the national importance it deserves. Not for me or for just a few people, but for all the multitude of people out there who are overwhelmed by their own health conditions and who need a helping hand. Working together we can make ripples of change.

“Individually, we are one drop. Together, we are an ocean.” Ryunosuke Satoro

 

End of page.

You may also like:

Written by: Kerry Ritchie, Programme Manager – Lived Experience, Integration and Engagement Hub Published: 14/04/2026

As part of our 20 year anniversary, Kerry shares her reflections on how far the ALLIANCE has come, our achievements, and our impact.

Continue reading
Written by: Sara Redmond, Chief Officer, the ALLIANCE Published: 02/04/2026

In her latest TFN column, our Chief Officer Sara Redmond reflects on 20 years since Scotland moved to put children at the centre of policy.

Continue reading
Written by: Hannah Buckingham, Senior External Affairs Adviser, Macmillan Cancer Support Published: 30/03/2026

Cancer care in Scotland is at a critical moment. Macmillan is calling for urgent action ahead of the parliamentary elections in May

Continue reading
Written by: Mhairi Campbell, Lecturer in Law at the University of the West of Scotland and is a lead author of Premenstrual Dysphoric Disorder and the Welfare State: Recommendations for Reform. She leads the teaching on social security law. Published: 27/03/2026

Mhairi Campbell reflects on Premenstrual Dysphoric Disorder (PMDD) not being recognised as having a severe impact on life.

Continue reading
Written by: Louise Hall, Pain Health & Wellbeing Coach, Pain Association Scotland Published: 11/03/2026

Louise Hall from Pain Association Scotland reflects on the event she delivered as part of Self Management Week 2025.

Continue reading
Written by: Lauren Ferrier, Events and Communications Officer and Jane Miller, Academy Programme Manager, the ALLIANCE and Gozie Joe-Adigwe, Digital Network Officer, the ALLIANCE and Rhona McMillan, Development Officer, the ALLIANCE Published: 20/02/2026

Read some reflections from ALLIANCE colleagues, who had the opportunity to sponsor and attend Scotland's Annual Human Rights Conference.

Continue reading
Back to all opinions